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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750926Generated: November 2, 2026

Benzaldehyde → 2,4-Di(prop-1-en-2-yl)dibenzo[b,d]thiophen-3-amine

https://huagongshe.com/reaction/1750926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
Reactant2,4-Dibromodibenzo[b,d]thiophen-3-amineHCID 58401040—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2,4-Di(prop-1-en-2-yl)dibenzo[b,d]thiophen-3-amineHCID 5840099695%

Reaction Steps

To a degassed toluene (200 mL), 2,4-dibromodibenzo[b,d]thiophen-3-amine (12.15 g, 34.0 mmol), 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (17.15 g, 102 mmol), benzaldehyde (3.61 g, 34.0 mmol), potassium phosphate (23.51 g, 102 mmol) dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (1.676 g, 4.08 mmol) and Pd2(dba)3 (0.935 g, 1.021 mmol) and water (20 mL) were sequentially added. The solution was refluxed for overnight in an atmosphere of nitrogen and then allowed to cool to room temperature. The reaction was diluted with ethyl acetate and the organic phase was separated from the aqueous phase. The organic phase was dried over sodium sulfate and the solvent was removed under vacuum. The product was chromatographed using silica gel with ethylacetate and hexanes as the eluent. The solvent was removed to give the title compound (9.0, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156870B2
Source datasetuspto-grants-2015_10
ORD IDord-03171f66983c42f68f9f6cbdfa382131
Source noteuspto-grants-2015_10